chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
115023061350230614CT18GENICpossibly homozygous51004568
115023100950231010A-1GENIChomozygous51004569
115023163950231640TC23GENIChomozygous51004570
115023179650231797AG23GENIChomozygous51004571
115023388850233889A-7GENICheterozygous51288550